AR099880A1 - NICOTINAMIDE DERIVATIVES AS TRPA1 MODULATORS - Google Patents
NICOTINAMIDE DERIVATIVES AS TRPA1 MODULATORSInfo
- Publication number
- AR099880A1 AR099880A1 ARP150100930A ARP150100930A AR099880A1 AR 099880 A1 AR099880 A1 AR 099880A1 AR P150100930 A ARP150100930 A AR P150100930A AR P150100930 A ARP150100930 A AR P150100930A AR 099880 A1 AR099880 A1 AR 099880A1
- Authority
- AR
- Argentina
- Prior art keywords
- trpa1
- nicotinamide derivatives
- modulators
- trpa1 modulators
- cycloalkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Abstract
Exhiben actividad moduladora de TRPA1 y que por lo tanto son útiles como moduladores de TRPA1. Reivindicación 1: Un compuesto caracterizado porque es de fórmula (1) ó (2) donde; R¹ es cicloalquilo C₄₋₆ o fenilo, donde dicho cicloalquilo C₄₋₆ o fenilo no está sustituido o está sustituido con 1 ó 2 sustituyente(s) donde cada uno es en forma independiente halógeno, alcoxi C₁₋₂, o CN; y R² es H o halógeno; o una sal farmacéuticamente aceptable del mismo.They exhibit modulatory activity of TRPA1 and are therefore useful as modulators of TRPA1. Claim 1: A compound characterized in that it is of formula (1) or (2) wherein; R¹ is C₄₋₆ cycloalkyl or phenyl, wherein said C₄₋₆ cycloalkyl or phenyl is not substituted or substituted with 1 or 2 substituent (s) where each is independently halogen, C₁₋₂ alkoxy, or CN; and R² is H or halogen; or a pharmaceutically acceptable salt thereof.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI20140092 | 2014-03-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR099880A1 true AR099880A1 (en) | 2016-08-24 |
Family
ID=53005579
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150100930A AR099880A1 (en) | 2014-03-28 | 2015-03-27 | NICOTINAMIDE DERIVATIVES AS TRPA1 MODULATORS |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR099880A1 (en) |
TW (1) | TW201620876A (en) |
WO (1) | WO2015144976A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2884922C (en) * | 2012-10-01 | 2020-11-10 | Orion Corporation | N-prop-2-ynyl carboxamide derivatives and their use as trpa1 antagonists |
CA3036571C (en) * | 2016-09-12 | 2023-10-03 | Neuralstem, Inc. | Amelioration of neural deficits associated with diabetes |
FR3114235A1 (en) | 2020-09-18 | 2022-03-25 | Université Grenoble Alpes | INHIBITION OF ASTROCYTIC TRPA1 CHANNEL AS A NEW NEUROPROTECTIVE THERAPEUTIC TARGET IN THE PRODROMAL PHASES OF ALZHEIMER'S DISEASE |
IT202100015098A1 (en) | 2021-06-09 | 2022-12-09 | Flonext S R L | TRPA1 CHANNEL ANTAGONIST COMPOUND FOR USE IN DEGENERATIVE DISEASES OF THE RETINA |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2280707A1 (en) * | 2008-05-05 | 2011-02-09 | Allergan, Inc. | Alpha2b and alpha2c agonists |
CA2884922C (en) * | 2012-10-01 | 2020-11-10 | Orion Corporation | N-prop-2-ynyl carboxamide derivatives and their use as trpa1 antagonists |
-
2015
- 2015-03-26 TW TW104109725A patent/TW201620876A/en unknown
- 2015-03-27 AR ARP150100930A patent/AR099880A1/en unknown
- 2015-03-27 WO PCT/FI2015/000012 patent/WO2015144976A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
TW201620876A (en) | 2016-06-16 |
WO2015144976A1 (en) | 2015-10-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |